微生物学免疫学进展
微生物學免疫學進展
미생물학면역학진전
Progress in Microbiology and Immunology
2015年
6期
61-64
,共4页
杨秋林(综述)%许丽芳(审校)
楊鞦林(綜述)%許麗芳(審校)
양추림(종술)%허려방(심교)
原虫%凋亡%Metacaspase
原蟲%凋亡%Metacaspase
원충%조망%Metacaspase
Protozoan%Apoptosis%Metacaspase
近年鉴定到Metacaspase、组织蛋白酶B、组织蛋白酶D、核酸酶( Endo G、Tatd 、Fen-1)等分子参与了原虫的凋亡,但不清楚这些分子在凋亡信号途径中的位置及相互关系。实验结果显示,Metacaspase可能具有调节原虫凋亡与细胞周期等功能,但是Metacaspase与Caspase的活化方式及作用底物不同,提示原虫存在与多细胞动物不同的凋亡途径;在疟原虫及利什曼原虫中发现其线粒体及溶酶体参与了其凋亡,提示原虫可能具有类似哺乳动物的溶酶体-线粒体凋亡途径;在利什曼原虫和锥虫中发现存在通过核酸酶而不依赖Caspase的凋亡途径。阐明原虫的凋亡机制有助于通过设计新药物诱导原虫凋亡来达到治疗疾病的目的。
近年鑒定到Metacaspase、組織蛋白酶B、組織蛋白酶D、覈痠酶( Endo G、Tatd 、Fen-1)等分子參與瞭原蟲的凋亡,但不清楚這些分子在凋亡信號途徑中的位置及相互關繫。實驗結果顯示,Metacaspase可能具有調節原蟲凋亡與細胞週期等功能,但是Metacaspase與Caspase的活化方式及作用底物不同,提示原蟲存在與多細胞動物不同的凋亡途徑;在瘧原蟲及利什曼原蟲中髮現其線粒體及溶酶體參與瞭其凋亡,提示原蟲可能具有類似哺乳動物的溶酶體-線粒體凋亡途徑;在利什曼原蟲和錐蟲中髮現存在通過覈痠酶而不依賴Caspase的凋亡途徑。闡明原蟲的凋亡機製有助于通過設計新藥物誘導原蟲凋亡來達到治療疾病的目的。
근년감정도Metacaspase、조직단백매B、조직단백매D、핵산매( Endo G、Tatd 、Fen-1)등분자삼여료원충적조망,단불청초저사분자재조망신호도경중적위치급상호관계。실험결과현시,Metacaspase가능구유조절원충조망여세포주기등공능,단시Metacaspase여Caspase적활화방식급작용저물불동,제시원충존재여다세포동물불동적조망도경;재학원충급리십만원충중발현기선립체급용매체삼여료기조망,제시원충가능구유유사포유동물적용매체-선립체조망도경;재리십만원충화추충중발현존재통과핵산매이불의뢰Caspase적조망도경。천명원충적조망궤제유조우통과설계신약물유도원충조망래체도치료질병적목적。
Recently, a number of molecules which are involved in the apoptosis in protozoa have been discovered, for ex-ample:metacaspase, cathepsin B and D, nuclease( Endo G, Tatd, Fen-1 et al) .So far the locations of these molecules in the signal pathway of protozoan apoptosis and the relationship associated to these molecules in the signal pathway have not been identified.The results of experiments showed that the activation mode is different between metacaspase and caspase. The substrates are also different for metacaspase and caspase.The results suggested that the apoptosis mechanism is different between protozoan and metazoan.Metacaspase has multifunction, for example: control of apoptosis, cell cycle and clear-ance of insoluble protein aggregates.The results of experiment showed that mitochondrial and lysosomal body are involved in the apoptosis in protozoan, possibly, there are mitochondrial-lysosomal body pathway and caspase-independent pathway which control the apoptosis in protozoan.Uncovering clearly the mechanism of apoptosis in protozoan is benefit for design of new drugs in prevention and treatment of diseases caused by the protozoa.